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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1619109생성일: 2026년 10월 25일

Triethylamine → N'-(3-Bromophenyl)tetrahydro-2H-thiopyran-4-carbohydrazide

https://huagongshe.com/reaction/1619109

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Bromophenylhydrazine hydrochlorideHCID 33757—
반응물Oxalyl chlorideHCID 65578—
반응물Tetrahydrothiopyran-4-carboxylic acidHCID 21598642—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N'-(3-Bromophenyl)tetrahydro-2H-thiopyran-4-carbohydrazideHCID 6695850860%

반응 단계

Oxalyl chloride (1.20 mL, 14.2 mmol) was added dropwise to a stirred solution of tetrahydro-2H-thiopyran-4-carboxylic acid (WO2007006732, 2.00 g, 13.7 mmol) in dichloromethane (25 mL). Then, two drops of N,N′-dimethylformamide were added and stirring was continued. After 1.5 hours, the resultant solution was added dropwise over 30 minutes to a stirred, cooled (ice-bath) solution of (3-bromophenyl)hydrazine hydrochloride (3.05 g, 13.7 mmol) and triethylamine (4.20 mL, 30.1 mmol) in dichloromethane (40 mL). After the addition, the mixture was warmed to room temperature and stirred for two hours. The mixture was then concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was washed with 4% aqueous sodium hydrogen carbonate solution, dried (MgSO4) and evaporated. The residue was triturated with diethyl ether and the solid was filtered and dried to give the title compound (2.57 g, 60%) as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08772288B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-0e8cfd6102fa4244b5597544d3bc83be
출처 메모uspto-grants-2014_07